Emergency Department-based Cervical Cancer Screening Through Self-sampling
Recruiting
N/A
Interventional Study
HPV
HPV Associated Cancers
HPV Cancers
Cervical Cancer Screening
Cervical Cancer (Early Detection)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 30 – 65
- Sex
- Female
- Study type
- Interventional
- Purpose
- Screening
- Participants needed
- 200 (estimated)
- Sponsor
- University of Rochester · Other
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About This Trial
This project will compare the uptake of cervical cancer screening through ED HPV sampling among patients presenting to the ED.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Cisgender women and transgender/non-binary individuals with a cervix,
* Age 30 - 65 years, and demonstrating decisional capacity to consent to participate with no known exclusion criteria present.
Exclusion Criteria:
* Past hysterectomy with cervical removal
* Known infectio…
Contacts